LC-NMR and LC-MS identification of an impurity in a novel antifungal drug icofungipen

J Pharm Biomed Anal. 2009 Aug 15;50(1):68-72. doi: 10.1016/j.jpba.2009.03.017. Epub 2009 Mar 25.

Abstract

Successful use of LC-NMR and LC-MS for rapid identification of an impurity in a novel antifungal drug icofungipen has been demonstrated. Complementary information obtained from the two methods made it possible to determine the structure of A1 prior to its isolation and purification. Stop-flow LC-NMR ((1)H and DQFCOSY), LC-MS and LC-MS/MS spectra have shown that A1 is structurally related to icofungipen. It was later isolated and prepared synthetically and its structure was corroborated by high-resolution NMR spectroscopy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antifungal Agents / chemistry*
  • Chromatography, Liquid / methods*
  • Cycloleucine / analogs & derivatives*
  • Cycloleucine / chemistry
  • Magnetic Resonance Spectroscopy / methods*
  • Mass Spectrometry / methods*

Substances

  • Antifungal Agents
  • Cycloleucine
  • 2-amino-4-methylenecyclopentane-1-carboxylic acid